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145 related items for PubMed ID: 15003568
1. Utilization of biotinylated diphenyl phosphonates for disclosure of serine proteases. Hawthorne S, Hamilton R, Walker BJ, Walker B. Anal Biochem; 2004 Mar 15; 326(2):273-5. PubMed ID: 15003568 [No Abstract] [Full Text] [Related]
2. Novel diphenyl esters of peptidyl alpha-aminoalkylphosphonates as inhibitors of chymotrypsin and subtilisin. Pietrusewicz E, Sieńczyk M, Oleksyszyn J. J Enzyme Inhib Med Chem; 2009 Dec 15; 24(6):1229-36. PubMed ID: 19912056 [Abstract] [Full Text] [Related]
3. Synthesis and kinetic studies of diphenyl 1-(N-peptidylamino)alkanephosphonate esters and their biotinylated derivatives as inhibitors of serine proteases and probes for lymphocyte granzymes. Abuelyaman AS, Jackson DS, Hudig D, Woodard SL, Powers JC. Arch Biochem Biophys; 1997 Aug 15; 344(2):271-80. PubMed ID: 9264539 [Abstract] [Full Text] [Related]
4. Tuning activity-based probe selectivity for serine proteases by on-resin 'click' construction of peptide diphenyl phosphonates. Serim S, Mayer SV, Verhelst SH. Org Biomol Chem; 2013 Sep 14; 11(34):5714-21. PubMed ID: 23884325 [Abstract] [Full Text] [Related]
5. Synthesis, kinetic evaluation, and utilization of a biotinylated dipeptide proline diphenyl phosphonate for the disclosure of dipeptidyl peptidase IV-like serine proteases. Gilmore BF, Carson L, McShane LL, Quinn D, Coulter WA, Walker B. Biochem Biophys Res Commun; 2006 Aug 18; 347(1):373-9. PubMed ID: 16824486 [Abstract] [Full Text] [Related]
6. Dipeptide proline diphenyl phosphonates are potent, irreversible inhibitors of seprase (FAPalpha). Gilmore BF, Lynas JF, Scott CJ, McGoohan C, Martin L, Walker B. Biochem Biophys Res Commun; 2006 Jul 28; 346(2):436-46. PubMed ID: 16769036 [Abstract] [Full Text] [Related]
7. alpha-Aminoalkylphosphonate di(chlorophenyl) esters as inhibitors of serine proteases. Boduszek B, Brown AD, Powers JC. J Enzyme Inhib; 1994 Jul 28; 8(3):147-58. PubMed ID: 7539484 [Abstract] [Full Text] [Related]
8. Phosphonic pseudopeptides as human neutrophil elastase inhibitors--a combinatorial approach. Sieńczyk M, Podgórski D, Błażejewska A, Kulbacka J, Saczko J, Oleksyszyn J. Bioorg Med Chem; 2011 Feb 01; 19(3):1277-84. PubMed ID: 21216608 [Abstract] [Full Text] [Related]
9. Selective chemical functional probes of granzymes A and B reveal granzyme B is a major effector of natural killer cell-mediated lysis of target cells. Mahrus S, Craik CS. Chem Biol; 2005 May 01; 12(5):567-77. PubMed ID: 15911377 [Abstract] [Full Text] [Related]
10. Discovery of inhibitors of the channel-activating protease prostasin (CAP1/PRSS8) utilizing structure-based design. Tully DC, Vidal A, Chatterjee AK, Williams JA, Roberts MJ, Petrassi HM, Spraggon G, Bursulaya B, Pacoma R, Shipway A, Schumacher AM, Danahay H, Harris JL. Bioorg Med Chem Lett; 2008 Nov 15; 18(22):5895-9. PubMed ID: 18752942 [Abstract] [Full Text] [Related]
11. A comparative study of antichymotryptic and anticholinesterase activity of organophosphorus quasi-substrate inhibitors. Rozengart EV. Dokl Biochem Biophys; 2008 Nov 15; 419():82-7. PubMed ID: 18505164 [No Abstract] [Full Text] [Related]
12. A Bisbenzamidine Phosphonate as a Janus-faced Inhibitor for Trypsin-like Serine Proteases. Häußler D, Scheidt T, Stirnberg M, Steinmetzer T, Gütschow M. ChemMedChem; 2015 Oct 15; 10(10):1641-6. PubMed ID: 26306030 [Abstract] [Full Text] [Related]